FDAJune 24, 2022device

Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

00887761977914

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04. — Recall Details · AllClear